This summer we will be participating in the Walk to End ALS.

In 2018 I lost my dad to ALS. In just 4 weeks after diagnosis he was sadly taken from us. This disease is dibiltating taking everything from you. From walking, talking, swallowing, eating and drinking, to not even being able to do simple tasks yourself like brushing your teeth. This disease is fatal and there is no cure. Help us by donating or joining us June 14th to walk to end ALS.

Now more than ever, the ALS community needs our support to provide hope and help to families affected by ALS/MND. That’s why we're joining thousands of others, a part of a passionate and motivated community to “walk” in celebration of hope and a world free of ALS, also known as Lou Gehrig’s Disease. Please consider supporting us and donating towards this important cause.

Your support will help to:

• create a better day-to-day reality for people and families living with ALS by providing community-based support throughout Manitoba as well as necessary medical equipment like wheelchairs, liftchairs, mobility aids and other items that increase safety in the home, at no cost to those who need them.
• further scientific progress by investing in the ALS Canada Research Program, which funds promising ALS research. This program provides peer-reviewed grants to researchers whose work has the greatest potential to advance the field of ALS. There’s been more progress made in ALS research in the last five years than over the last century – we need to keep building on this momentum.

Join us in making a difference. Please consider donating to this fundraising page as we work towards a world free of ALS/MND.

Your support is needed now more than ever - we are stronger together!